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ClearPoint Neuro, Inc. Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

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ClearPoint Neuro, Inc.

Irvine, California, United States
Issue DateJuly 25, 2018
FEI Number3002838670
CountryUnited States
Status
No Warning Letter
Product Type
Devices
ClearPoint Neuro, Inc. FDA Form 483, Irvine, California, July 25, 2018